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      Actinide-based single-molecule magnets: alone or in a group?

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          Abstract

          This review presents a survey of representative mononuclear and multinuclear actinide SMMs to look back at how far we have come, trying to seek out a feasible strategy for top-performing An-SMMs.

          Abstract

          In recent years, very significant progress has been made in single-molecule magnets (SMMs), and one of the major milestone works is the hysteresis blocking temperature beyond the boiling point of liquid nitrogen. As increasingly abundant experimental and theoretical cases are studied, our understanding of how to construct high-performance rare-earth SMMs is becoming clearer, while few good SMMs have been reported for actinides that possess stronger spin–orbital coupling than rare earths. Recently, attempts to replicate the successful strategy on rare-earth SMMs to actinides have proven to be a failure, or at least frustrating, with the main reason being the stronger covalent contribution in the actinide-ligand bonds. In this review, the progress on actinide SMMs is summarized to look back at how far we have come and try to find possible routes forward.

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          Most cited references63

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          Molecular spintronics using single-molecule magnets.

          A revolution in electronics is in view, with the contemporary evolution of the two novel disciplines of spintronics and molecular electronics. A fundamental link between these two fields can be established using molecular magnetic materials and, in particular, single-molecule magnets. Here, we review the first progress in the resulting field, molecular spintronics, which will enable the manipulation of spin and charges in electronic devices containing one or more molecules. We discuss the advantages over more conventional materials, and the potential applications in information storage and processing. We also outline current challenges in the field, and propose convenient schemes to overcome them.
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            Lanthanide double-decker complexes functioning as magnets at the single-molecular level.

            Double-decker phthalocyanine complexes with Tb3+ or Dy3+ showed slow magnetization relaxation as a single-molecular property. The temperature ranges in which the behavior was observed were far higher than that of the transition-metal-cluster single-molecule magnets (SMMs). The significant temperature rise results from a mechanism in the relaxation process different from that in the transition-metal-cluster SMMs. The effective energy barrier for reversal of the magnetic moment is determined by the ligand field around a lanthanide ion, which gives the lowest degenerate substate a large |Jz| value and large energy separations from the rest of the substates in the ground-state multiplets.
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              Magnetic hysteresis up to 80 kelvin in a dysprosium metallocene single-molecule magnet

              Single-molecule magnets (SMMs) containing only one metal center may represent the lower size limit for molecule-based magnetic information storage materials. Their current drawback is that all SMMs require liquid-helium cooling to show magnetic memory effects. We now report a chemical strategy to access the dysprosium metallocene cation [(CpiPr5)Dy(Cp*)]+ (CpiPr5 = penta-iso-propylcyclopentadienyl, Cp* = pentamethylcyclopentadienyl), which displays magnetic hysteresis above liquid-nitrogen temperatures. An effective energy barrier to reversal of the magnetization of Ueff = 1,541 cm–1 is also measured. The magnetic blocking temperature of TB = 80 K for this cation overcomes an essential barrier towards the development of nanomagnet devices that function at practical temperatures.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                ICFNAW
                Inorganic Chemistry Frontiers
                Inorg. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1553
                June 27 2023
                2023
                : 10
                : 13
                : 3742-3755
                Affiliations
                [1 ]Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Xiyuan Avenue 2006, Chengdu, 611731, China
                [2 ]Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, Sun Yat-Sen University, Guangzhou 510006, China
                Article
                10.1039/D3QI00523B
                807c6118-e03c-4f4f-80cf-b7ebc668d228
                © 2023

                http://rsc.li/journals-terms-of-use

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